ethyl 2-(3,3-dimethylbutanoylamino)-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate | 1028931-59-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并吡喃类
• 英文名称: ethyl 2-(3,3-dimethylbutanoylamino)-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate
• CAS: 1028931-59-0
• 化学式: C₁₆H₂₃NO₄S
• 分子量: 325.429
• InChiKey: GRKUOPJFFNMDQC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  22
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  92.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  ethyl 2-(3,3-dimethylbutanoylamino)-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate 在 potassium hydroxide 作用下， 以 乙醇 为溶剂， 生成 C₁₄H₁₉NO₄S
  参考文献：
  名称：

  Structure–activity relationships of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists and their analgesic action

  摘要：

  SAR studies were performed ona series of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists. Starting from a HTS hit both potency and selectivity could be improved. Modifications to the thiophene fusion and C-3 amides were studied. A representative compound 3t produced analgesia when dosed orally in inflammatory pain models of writhing and carrageenan-induced allodynia. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.087
• 作为产物：
  描述：

  四氢吡喃酮 在 吡啶 、 1,2,3,4,5,6,7,8-八硫杂环辛烷 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 ethyl 2-(3,3-dimethylbutanoylamino)-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate
  参考文献：
  名称：

  Structure–activity relationships of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists and their analgesic action

  摘要：

  SAR studies were performed ona series of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists. Starting from a HTS hit both potency and selectivity could be improved. Modifications to the thiophene fusion and C-3 amides were studied. A representative compound 3t produced analgesia when dosed orally in inflammatory pain models of writhing and carrageenan-induced allodynia. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.087

文献信息

• Structure–activity relationships of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists and their analgesic action
  作者：Yithachu Thur、Amit Bhalerao、Zaki Munshi、Nisha Pansare、Klaus Mann、Guido Hanauer、Hans-Peter Kley、Sandra Nappe、Cornelia Weiss-Haljiti、Claude Ostermann、Christof Zitt、Michaela Schaefer、Dibyendu Mondal、Afsar Ali Siddiki、Velavan Armugam、Vinod Gudaghe、Mahendra Gupta、Pramila Rayudu、Frank M. Dautzenberg、Koushik Das Sarma

  DOI：10.1016/j.bmcl.2012.10.087

  日期：2012.12

  SAR studies were performed ona series of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists. Starting from a HTS hit both potency and selectivity could be improved. Modifications to the thiophene fusion and C-3 amides were studied. A representative compound 3t produced analgesia when dosed orally in inflammatory pain models of writhing and carrageenan-induced allodynia. (C) 2012 Elsevier Ltd. All rights reserved.